35 yo F admitted with preterm premature rupture of...

35 YO F ADMITTED WITH PRETERM PREMATURE

RUPTURE OF MEMBRANES

Anila Bindal, MD

December 3, 2015

• G5P0403 at 22w2d by Fetal US

• Initially presented to Indiana after “large gush of fluid”

• Admitted for expectant management • Received antibiotics • Started on 17-hydroxyprogesterone

• Transferred to UCMC because nearing variability • Confirmed leakage of fluid, +nitrazine, +ferning, good fetal movement • Absent vaginal bleeding, contractions

PMH:

•Preterm delivery x 4

• 1 neonatal demise at 22 wks

PSH: none

FH: + Diabetes

NKDA

Meds: PNV

SH:

•Works as a waitress, has not been working during pregnancy

•No tobacco, ETOH, or illicits

•Has 3 sons

ROS • GEN: denies fevers, chills, night sweats; +5lb weight loss a few weeks ago

• HEENT: denies vision problems; +new BL hearing loss 3-4 years ago (uses bilateral hearing aids), underdeveloped phonation

• RESP: denies SOB

• CV: denies CP, orthopnea

• GI: denies nausea, emesis, constipation, diarrhea; normal appetite

• DERM: denies rashes

• MSK: denies weakness, edema, neuropathy

• PSYCH: denies depression

Physical Exam Temp: 36.5 (97.7) BP: 97/55 HR: 91 RR: 18 SaO2: 100% RA Ht: 149.9cm (4’11”) Wt 39kg (86lb) BMI 17.4

GEN: Thin, Caucasian, NAD HEENT: EOMI, no scleral icterus, PERRLA, MMM, no thyromegaly CV: RRR, nml S1/S2 PULM: CTA B ABD: NT, +gravid EXT: 2+ DP/radial pulses, no edema DERM: no acanthosis nigricans NEURO: alert, oriented, no tremor PSYCH: normal affect, pleasant

Ca 10.6

128 91

4.9 0.5

394

12

15

6.7 6.9 226

13

56

7

0.2

3.1 5.5

Labs

+ketones

• No h/o diabetes (including GDM) • Received prenatal care throughout pregnancy • Had not seen a doctor since last pregnancy (12 years ago) • Eats one full meal (dinner); otherwise snacks throughout the day • Diet includes meats, potatoes, vegetables

Diabetes on maternal side: • Mother (Type I, diagnosed age 26, uses bilateral hearing aids) • MGM (unknown type, diagnosed ?18 years ago) • MGGM (unknown type)

Does she possibly have MIDD? What is MIDD?

What is MIDD?

Maternally Inherited Diabetes and Deafness

• Mitochondrial disease

• Diabetes accompanied by hearing loss

• Usually develops in mid-adulthood

Murphy et al, Diabetic Medicine 2008

Other names for MIDD

• Ballinger-Wallace syndrome

• Type II DM with deafness

• Maternally-transmitted diabetes-deafness syndrome

• Mitochondrial inherited diabetes and deafness

• NIDDM with deafness

Other Labs/Studies?

HbA1c 8.5% BG 185 Ketones: 5.34 C-peptide 0.19

GAD65 Ab neg Insulin Ab neg ZnT8 neg IAT2 neg

Cortisol (@0811): 25.4 TSH 0.25 0.67

TTE WNL (LVEF 60%)

Facts about MIDD • First described in 1992

• ~1% of all diabetes cases (esp Japanese but found worldwide)

• Egg cells (but not sperm cells) contribute Mitochondrial DNA to developing embryo both M/F affected but only F pass it on

Donovan et al, JCEM 2006

• Mutations in MT-TL1 (leucine), MT-TK (lysine), MT-TE genes (glutamic acid)

• Most commonly AG at 3243 in tRNA Leucine gene

• Same mutation m.3243A>G linked to MELAS (myopathy, encephalopathy, lactic acidosis, strokelike episodes), which has a more severe phenotype and worse prognosis

• Enhanced degradation of mitochondrial DNA-encoded proteins

Reduction of functional respiratory enzyme complexes and reduced ATP generation

Altered ATP:ADP may result in impaired insulin secretion and beta-cell apoptosis

Features of MIDD • Hearing loss • Bilateral, progressive • Sensorineural, higher frequency • Usually age 20-30, mean age onset 33-34 yo • Often before DM onset

• Diabetes • insulin sensitivity intact but β-cell dysfunction, loss of β-cell mass insulinopenia • Mean age onset mid to late-30’s • Likely associated with progressive reduction of oxidative phosphorylation and

implicating glucose-sensing mechanism of β-cells

• Thin (BMI < 20) • Especially those requiring insulin early on

• Short stature • Due to GHRH deficiency Donovan et al, JCEM 2006

Features of MIDD • CV disease • Especially cardiac conduction abnormalities (WPW, Afib) • Can also have cardiomyopathy/CHF • LVH in absence of HTN seen 4x more • Cardiac autonomic neuropathy

• Advanced microvascular complications: • Renal disease: • Proteinuria, especially FSGS • Often misdiagnosed as Alport syndrome

• Neuropathy

Guillausseau et al, Annal Int Med, 2001 Donovan et al, JCEM 2006

Murphy et al, Diabetic Medicine 2008

Other Features of MIDD • Weakness in proximal muscles: cramps or weakness, esp during exercise • Muscle biopsy shows ragged-red fibers typical of mitochondrial

myopathy • Higher lactate levels post-exercise

• GI symptoms • Especially constipation or pseudo-obstruction

• Neuropsychiatric symptoms • Depression, schizophrenia, phobias

Picture from Carvalho et al, Archives of Neuropsychiatry, 2004

Characteristic Macular Retinal Dystrophy: usually without vision problems

Pigment builds up in the cells of the macula

Ogun et al, Neurology 2012 Less Diabetic Retinopathy than seen in T2DM

Phenotype of MIDD

• Wide variety in phenotypic expression

• Heteroplasmy: A mix of wild-type and mutant DNA in the same cell

• Severity of MIDD features associated with percentage of mutated mitochondrial DNA • Blood may show negative result despite presence of mutation in other

tissues because leukocytes have lowest level of heteroplasmy • Consider checking urine and/or buccal samples

• Symptoms often more severe in men

• Penetrance of diabetes in offspring is 85% by 70 yo

Murphy et al, Diabetic Medicine 2008 Donovan et al, JCEM 2006

Treatment of MIDD •Metformin discouraged as more likely to cause lactic acidosis

• First-line includes secretagogues (i.e. glyburide)

•Mean duration of DM before insulin dependence: 2-4 years • Continue taking carbs when ill (stroke-like symptoms when lacked carbs)

•Coenzyme Q10

• ?Avoid statins due to reduced CoQ10 levels

•Hearing aids or cochlear implants for hearing loss

Murphy et al, Diabetic Medicine 2008 Donovan et al, JCEM 2006

• CoQ10 is an electron carrier in the respiratory chain used in mitochondrial oxidative phosphorylation which in turn synthesizes ATP

• High amounts of CoQ10 in tissues with high energy requirements

• Also acts as antioxidant

• Mutant mitochondria show enhanced release of free radicals and impairment of mitochondrial respiratory chain

CoQ10 Repletion? • Few studies done: small, open

label, not subject to double-blinding or randomization

• Some suggest delayed hearing loss, enhanced insulin secretion, reduced lactate levels post-exercise

• Some suggest improved myopathy symptoms, improved painful neuropathy and/or CHF

• Others report no difference Chong et al, Practical Diabetes 2014

Murphy et al, Diabetic Medicine 2008

Other medication considerations in MIDD:

•Tetracyclines

•Chloramphenicol

•Phenytoin

•Valproate

•HMG CoA Reductase Inhibitors

•Antiretrovirals

MIDD During Pregnancy

•Placenta accreta

•Preterm labor

•PPROM

•Higher miscarriage rate

•Magnesium sulfate should be avoided! • Competes with calcium in mitochondrial membranes and may

exacerbate muscle damage

Donovan et al, JCEM 2006

Neonatology

Back to our patient…

•Treated for DKA

•Optholmalogy consult: eyes WNL

•Continue pregnancy or terminate? • Can choose to defer plan until 24 weeks at which point if she

chooses to terminate, she would have to do so in another state

Maternally inherited diabetes and deafness

Wolfram Syndrome

RCAD Renal cysts and diabetes

Optic atrophy

Retinitis Pigmentosa

Prader Willi Syndrome

Alstrom Syndrome Bardet-Biedl Syndrome

Type A insulin Resistance Leprechaunism Rabson-Mendenhall Syndrome Partial Lipodystrophy Mandibular Dysplasia with Deafness and Progeroid features (MDP/POLD1) Syndrome Hattersley et al, Diabetes Genes

Hattersley et al, Diabetes Genes

Our patient…

• Fetal Echo WNL except possible PAC’s

•No signs of preterm labor

•Plan for patient to be hospitalized until delivers

Patient’s course… • 24 days after admission, at GA 25w4d, patient went into active

preterm labor • Spontaneous NSVD • Failure of attempted manual extraction of the placenta D&C

• Baby in NICU

• Patient discharged 5 days later

Follow-up

• Patient asked to follow-up with UCMC Endo clinic at least once but reports she prefers to follow in Indiana due to insurance issues

• Tried to call several times but patient not responsive

• Geneticist called patient twice about genetic testing results and official diagnosis, but patient not responsive

• Baby still in NICU with grade IV IVH and patient has been visiting

References • Carvalho AAS, Lima UWP, Valiente RA. Statin and fibrate-associated myopathy: study of eight patients.

Archives of Neuropsychiatry. 2004, June;62(2)257-261

• Chong ZM, Jones GC. Drug Notes: Coenzyme Q10. Practical Diabetes. 2014;31(4):173-174a

• Donovan LE, Severin NE. Maternally Inherited Diabetes and Deafness in a North American Kindred: Tips for Making the Diagnosis and Review of Unique Management Issues. JCEM. 2006, Dec; 91(12):4737-42

• Guillausseau PJ, Massin P, Dubois-LaForgue D, et al. Maternally Inherited Diabetes and Deafness: A Multicenter Study. Ann Intern Med. 2001;134:721-728

• Hattersley A, Shepherd M, Flanagan S. Other Rare Types of Diabetes. Diabetes Genes. [Online]. Available: http://www.diabetesgenes.org/content/information-known-types-rare-diabetes. [Date accessed] November 29, 2015.

• Murphy R, Turnbull DM, Walker M, Hattersley AT. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation. Diabetic Medicine. 2008, Apr;25(4):383-399

• Naing A, Kenchaiah M, Krishnan B, Mir F, Charnley A, Egan C, Bano G. Maternally inherited diabetes and deafness (MIDD): Diagnosis and management. Journal of Diabetes and its Complications. 2014, July;28(4):542-546

• Ogun O, Sheldon C, Barton JJS. Pearls & Oy-sters: Maternally Inherited Diabetes and Deafness presenting with Ptosis and Macular Pattern Dystrophy. Neurology. 2012, Aug; 79(6):54-56